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Home >> Signaling Pathways >> GPCR/G protein >> Adrenergic Receptor

Adrenergic Receptor

Adrenergic receptor is a class of G protein-coupled receptors that are targets of the catecholamines, especially norepinephrine and epinephrine.

Products for  Adrenergic Receptor

  1. Cat.No. Product Name Information
  2. GC12626 Cimaterol β-Adrenergic agonist Cimaterol Chemical Structure
  3. GC45826 Cimaterol-d7 An internal standard for the quantification of cimaterol Cimaterol-d7 Chemical Structure
  4. GC62897 Cimbuterol-D9 Cimbuterol-D9 is the deuterium labeled Cimbuterol. Cimbuterol-D9 Chemical Structure
  5. GC15218 Cirazoline hydrochloride α1 agonist Cirazoline hydrochloride Chemical Structure
  6. GC12226 Cisatracurium Besylate Neuromuscular-blocking drug Cisatracurium Besylate Chemical Structure
  7. GC43276 CL 316,243 (disodium salt)

    A murine-selective β3 adrenoceptor agonist

     CL 316,243 (disodium salt) Chemical Structure
  8. GC12778 Clenbuterol (hydrochloride) sympathomimetic β2-adrenoceptor agonist used as a bronchodilator in the treatment of pulmonary diseases Clenbuterol (hydrochloride) Chemical Structure
  9. GC68418 Clenbuterol-d9 Clenbuterol-d9 Chemical Structure
  10. GC62900 Clenproperol-D7 Clenproperol-D7 is the deuterium labeled Clenproperol. Clenproperol-D7 Chemical Structure
  11. GC60717 Clonidine Clonidine is an alpha 2-adrenergic agonist. Clonidine Chemical Structure
  12. GC14032 Clonidine HCl Clonidine HCl is an agonist of α2-adrenoceptor and potent antihypertensive agent. Clonidine HCl Chemical Structure
  13. GC12949 Clorprenaline HCL Clorprenaline HCL is a β2-adrenergic receptor agonist that is implicated in bronchial expansion. Clorprenaline HCL Chemical Structure
  14. GC30665 D2343 D2343 is a β2-adrenoceptor agonist and also is an α1- adrenoceptor inhibitor. D2343 Chemical Structure
  15. GC38762 Dabuzalgron Dabuzalgron (Ro 115-1240) is an orally active and selective α-1A adrenergic receptor agonist for the treatment of urinary incontinence. Dabuzalgron Chemical Structure
  16. GC30188 Dapiprazole hydrochloride An α-adrenergic receptor antagonist Dapiprazole hydrochloride Chemical Structure
  17. GC65955 Denopamine Denopamine ((R)-(-)-Denopamine) is an orally active, selective β1-adrenergic agonist. Denopamine prolongs survival in a murine model of congestive heart failure induced by viral myocarditis: suppression of tumor necrosis factor-α production in the heart. Cardiovascular effects. Denopamine Chemical Structure
  18. GC31468 Deriglidole (SL 86-0715) Deriglidole (SL 86-0715) is a peripheral adrenoceptor antagonist with a high affinity for α2-adrenoceptors. Deriglidole (SL 86-0715) Chemical Structure
  19. GC17197 Detomidine α2-adrenergic agonist Detomidine Chemical Structure
  20. GC17081 Detomidine HCl Detomidine HCl, an imidazole derivative, is a potent α2-adrenergic agonist. Detomidine HCl Chemical Structure
  21. GC17494 Dexmedetomidine

    An α2-adrenergic receptor agonist

     Dexmedetomidine Chemical Structure
  22. GC10750 Dexmedetomidine HCl Dexmedetomidine HCl ((+)-Medetomidine hydrochloride) is a potent, selective and orally active agonist of α2-adrenoceptor, with a Ki of 1.08 nM. Dexmedetomidine HCl Chemical Structure
  23. GC60764 Diacetolol D7 Diacetolol D7 is a deuterium labeled Diacetolol. Diacetolol D7 Chemical Structure
  24. GC60767 Dibenamine hydrochloride Dibenamine hydrochloride is a competitive and irreversible?adrenergic blocking agent and?is known to modify the pharmacological effects of epinephrine. Dibenamine hydrochloride Chemical Structure
  25. GC38527 Dicentrine Dicentrine is a natural product isolated from the plant Lindera megaphylla with antihypertensive effect. Dicentrine Chemical Structure
  26. GC13256 Dihydroergocristine mesylate 5-HT receptor antagonist and partial agonist of adrenergic and dopaminergic receptors Dihydroergocristine mesylate Chemical Structure
  27. GC13378 DL-Adrenaline Adrenergic receptor agonist DL-Adrenaline Chemical Structure
  28. GC39257 DL-Norepinephrine hydrochloride DL-Norepinephrine hydrochloride is a synthetic phenylethylamine that mimics the sympathomimetic actions of the endogenous norepinephrine．DL-Norepinephrine hydrochloride is a neurotransmitter targets α1 and β1 adrenoceptors, has an increasing effect on subendocardial oxygen tension. DL-Norepinephrine hydrochloride Chemical Structure
  29. GC35891 Dobutamine hydrochloride Dobutamine hydrochloride is a synthetic catecholamine that acts on α1-AR, β1-AR, β2-AR (α-1, β-1 andβ-2 adrenoceptors). Dobutamine hydrochloride Chemical Structure
  30. GC32627 Dopexamine hydrochloride (FPL60278AR) Dopexamine hydrochloride (FPL60278AR) is a β2 adrenergic receptor agonist. Dopexamine hydrochloride (FPL60278AR) Chemical Structure
  31. GC13447 Doxazosin Quinazoline-derivative that selectively antagonizes postsynaptic α1-adrenergic receptors Doxazosin Chemical Structure
  32. GC60790 Doxazosin D8 Doxazosin D8 (UK 33274 D8) is a deuterium labeled Doxazosin (UK 33274). Doxazosin D8 Chemical Structure
  33. GC13443 Doxazosin Mesylate α1-adrenergic receptor antagonist Doxazosin Mesylate Chemical Structure
  34. GC12042 DSP-4 DSP-4 is a highly and selective adrenergic neurotoxin. DSP-4 Chemical Structure
  35. GC32547 Ecastolol Ecastolol is a beta adrenergic receptor antagonist, with antianginal activities. Ecastolol Chemical Structure
  36. GC15672 Efaroxan hydrochloride α2 adrenoceptor antagonist and imidazoline I1 receptor ligand Efaroxan hydrochloride Chemical Structure
  37. GC31378 Epanolol (Visacor) Epanolol (Visacor) (Visacor; ICI141292) is a potent β-adrenoceptor partial agonist with a greater affinity for β1- than β2-adrenoceptors. Epanolol (Visacor) Chemical Structure
  38. GC13393 Epinephrine Bitartrate Adrenergic receptor agonist Epinephrine Bitartrate Chemical Structure
  39. GC15698 Epinephrine HCl Adrenergic receptor agonist Epinephrine HCl Chemical Structure
  40. GC25385 Esmolol Esmolol is a cardioselective beta1 receptor blocker with rapid onset, a very short duration of action, and no significant intrinsic sympathomimetic or membrane stabilising activity at therapeutic dosages. Esmolol Chemical Structure
  41. GC14968 Esmolol HCl Esmolol HCl is a beta adrenergic receptor blocker. Esmolol HCl Chemical Structure
  42. GC32418 Falintolol, (Z)- Falintolol, (Z)-, a new β-adrenergic antagonist, is characterized by the presence of an oxime function. Falintolol, (Z)- Chemical Structure
  43. GC18086 Fendiline (hydrochloride) α2-adrenergic receptor antagonist Fendiline (hydrochloride) Chemical Structure
  44. GC31271 Fenmetozole Tosylate Fenmetozole Tosylate is an antagonist of the actions of ethanol, also antagonizes α2-adrenergic receptor, and acts as an antidepressant drug. Fenmetozole Tosylate Chemical Structure
  45. GC25412 Fenoterol Fenoterol (Phenoterol) is a β2 adrenoreceptor agonist with bronchodilator activity. Fenoterol Chemical Structure
  46. GC43661 Fenoterol (hydrobromide) Fenoterol is an analytical reference standard categorized as a β2-adrenergic receptor agonist. Fenoterol (hydrobromide) Chemical Structure
  47. GC31750 Fenspiride Hydrochloride Fenspiride Hydrochloride Chemical Structure
  48. GC30679 Fiduxosin Fiduxosin is a potent α1-adrenoceptor antagonist, with Ki of 0.160 nM, 24.9 nM, and 0.920 nM for α1a-, α1b-, and α1d-adrenoceptors, respectively. Fiduxosin Chemical Structure
  49. GC15918 Formoterol Hemifumarate Potent, selective and long-acting β2-adrenoceptor agonist Formoterol Hemifumarate Chemical Structure
  50. GC11385 G-Protein antagonist peptide Inhibits G protein activation by GPCRs G-Protein antagonist peptide Chemical Structure
  51. GC41486 Glaucine Glaucine is an alkaloid originally isolated from G. Glaucine Chemical Structure
  52. GN10104 Gramine Gramine Chemical Structure
  53. GC25484 Guanabenz Guanabenz (GBZ, GA, Wytensin, Wy-8678,BR-750) is an orally active central alpha 2-adrenoceptor (α2 adrenergic receptor) agonist with antihypertensive action. Guanabenz Chemical Structure
  54. GC13302 Guanabenz (hydrochloride) α2-adrenergic receptor agonist Guanabenz (hydrochloride) Chemical Structure
  55. GC16839 Guanabenz Acetate α2-adrenergic receptor agonist Guanabenz Acetate Chemical Structure
  56. GC14813 Guanfacine selective α2A receptor agonist Guanfacine Chemical Structure
  57. GC12132 Guanfacine hydrochloride An α2-adrenergic receptor agonist Guanfacine hydrochloride Chemical Structure
  58. GC32662 Guanoxabenz (Hydroxyguanabenz) Guanoxabenz (Hydroxyguanabenz) is an α2 adrenergic receptor agonist, with a Ki of 4000 nM and the fully activated form 40 nM for an α2A adrenoceptor. Guanoxabenz (Hydroxyguanabenz) Chemical Structure
  59. GC61882 Guanoxabenz hydrochloride Guanoxabenz (Hydroxyguanabenz) hydrochloride is an α2 adrenergic receptor agonist, with a Ki of 4000 nM and the fully activated form 40 nM for an α2A adrenoceptor. Guanoxabenz hydrochloride Chemical Structure
  60. GC15384 Harmane endogenous ligand for imidazoline binding sites Harmane Chemical Structure
  61. GC12206 HEAT hydrochloride α1-adrenoceptor antagonist HEAT hydrochloride Chemical Structure
  62. GC38099 Higenamine Higenamine (Norcoclaurine), a β2-AR agonist, is a key component of the Chinese herb aconite root that prescribes for treating symptoms of heart failure in the oriental Asian countries. Higenamine Chemical Structure
  63. GC38237 Higenamine hydrochloride Higenamine hydrochloride (Norcoclaurine hydrochloride), a β2-AR agonist, is a key component of the Chinese herb aconite root that prescribes for treating symptoms of heart failure in the oriental Asian countries. Higenamine hydrochloride Chemical Structure
  64. GC12243 HOKU-81 HOKU-81 Chemical Structure
  65. GC36266 Hydrocortisone 17-butyrate Hydrocortisone 17-butyrate is an adrenocortico hormone Hydrocortisone 17-butyrate Chemical Structure
  66. GC43877 Hydroxy Bupropion Buproprion is an inhibitor of the reuptake of dopamine and norepinephrine and is also an antagonist of neuronal acetylcholine nicotinic receptors. Hydroxy Bupropion Chemical Structure
  67. GC14033 ICI 118,551 hydrochloride

    Highly selective β2 adrenergic receptor antagonist

     ICI 118,551 hydrochloride Chemical Structure
  68. GC16547 ICI 215,001 hydrochloride active metabolite of ZD 7114 ICI 215,001 hydrochloride Chemical Structure
  69. GC12761 ICI 89406 β-adrenergic antagonist ICI 89406 Chemical Structure
  70. GC38192 Idazoxan hydrochloride Idazoxan hydrochloride Chemical Structure
  71. GC15813 Idazoxan hydrochloride

    Idazoxan hydrochloride (RX 781094 hydrochloride) is an α2-adrenoceptor antagonist and also an antagonist of imidazoline receptors (IRs). 

     Idazoxan hydrochloride Chemical Structure
  72. GC11077 Imiloxan hydrochloride α2-adrenoceptor antagonist Imiloxan hydrochloride Chemical Structure
  73. GC33705 Imoxiterol (RP 58802B) Imoxiterol (RP 58802B) (RP 58802B) is a β-adrenergic agonist. Imoxiterol (RP 58802B) Chemical Structure
  74. GC13808 Indacaterol A long-acting β2-adrenergic receptor agonist Indacaterol Chemical Structure
  75. GC11130 Indacaterol Maleate Ultra-long-acting β-adrenoceptor agonist Indacaterol Maleate Chemical Structure
  76. GC32512 Indanidine Indanidine is an alpha-adrenergic agonist. Indanidine Chemical Structure
  77. GC30391 Indoramin D5 (Indoramine D5) Indoramin D5 (Indoramine D5) is deuterium labeled Indoramin, which is a piperidine antiadrenergic agent. Indoramin D5 (Indoramine D5) Chemical Structure
  78. GC64514 Isometheptene mucate Isometheptene mucate Chemical Structure
  79. GC11029 Isoprenaline HCl Isoprenaline (Isoproterenol) hydrochloride is a non-selective, orally active β-adrenergic receptor agonist. Isoprenaline HCl Chemical Structure
  80. GC17998 Isoxsuprine (hydrochloride) β-adrenergic receptor modulator Isoxsuprine (hydrochloride) Chemical Structure
  81. GC30434 Ivabradine D3 Hydrochloride An internal standard for the quantification of ivabradine Ivabradine D3 Hydrochloride Chemical Structure
  82. GC34289 Ivabradine D6 hydrochloride Ivabradine D6 hydrochloride Chemical Structure
  83. GC10194 Ivabradine HCl Ivabradine HCl is a potent and orally active HCN (hyperpolarization-activated cyclic nucleotide-gated) channel blocker that inhibits the cardiac pacemaker current (If). Ivabradine HCl Chemical Structure
  84. GC17884 JP 1302 dihydrochloride α2C-adrenoceptor antagonist JP 1302 dihydrochloride Chemical Structure
  85. GC43932 JP-1302 (hydrochloride) JP-1302 (hydrochloride) is a selective, high affinity antagonist of the alpha2C-adrenoceptor (α2C-adrenoceptor), with a Kb value (antagonist activity) of 16 nM and a Ki (binding affinity) value of 28 nM. JP-1302 (hydrochloride) Chemical Structure
  86. GC31329 Ko-3290 Ko-3290 is an antagonist of β-adrenoceptor, with cardioselectivity and antilipolytic effects in animals. Ko-3290 Chemical Structure
  87. GC36413 L-(-)-α-Methyldopa hydrate L-(-)-α-Methyldopa hydrate (L-(-)-α-L-(-)-α-Methyldopa hydrate), a potent antihyoertensive agent, is an alpha-adrenergic agonist (selective for α2-adrenergic receptors). L-(-)-α-Methyldopa hydrate Chemical Structure
  88. GC16401 L-(-)-α-Methyldopa hydrochloride L-(-)-α-Methyldopa hydrochloride (L-(-)-α-L-(-)-α-Methyldopa hydrochloride) hydrochloride, a potent antihyoertensive agent, is an alpha-adrenergic agonist (selective for α2-adrenergic receptors). L-(-)-α-Methyldopa hydrochloride Chemical Structure
  89. GC16939 L-748,337 Competitive β3-adrenoceptor antagonist L-748,337 Chemical Structure
  90. GC15743 L-755,507 β3 adrenergic receptor agonist L-755,507 Chemical Structure
  91. GC32670 L-765314 L-765314 is a potent and selective α1b adrenergic receptor antagonist with Kis of 5.4 nM and 2.0 nM for rat and human α1b adrenergic receptor, respectively. L-765314 Chemical Structure
  92. GC33410 L-771688 L-771688 is a highly selective α1A-Adrenoceptor antagonist with a Ki of 0.43±0.02 nM. L-771688 Chemical Structure
  93. GC14816 L-Adrenaline An adrenergic receptor agonist L-Adrenaline Chemical Structure
  94. GC17319 L-Phenylephrine (R)-(-)-L-Phenylephrine is a selective α1-adrenoceptor agonist primarily used as a decongestant. L-Phenylephrine Chemical Structure
  95. GC64143 Labetalol Labetalol (AH5158) is an orally active selective α1- and non-selective β-adrenergic receptors competitive antagonist. Labetalol Chemical Structure
  96. GC10887 Labetalol HCl Labetalol HCl is a mixed alpha/beta adrenergic antagonist that is used to treat high blood pressure. Labetalol HCl Chemical Structure
  97. GC36422 Landiolol hydrochloride Landiolol hydrochloride (ONO1101 hydrochloride) is a highly beta1 selective ultra-short acting beta-blocker (β1/β2 selectivity?=?255:1, a half-life of 4?min)， acts as an adrenoceptor antagonist. Landiolol hydrochloride Chemical Structure
  98. GC17974 Latrepirdine dihydrochloride Latrepirdine is a neuroactive compound with antagonist activity at histaminergic, α-adrenergic, and serotonergic receptors. Latrepirdine dihydrochloride Chemical Structure
  99. GC36441 Levalbuterol tartrate Levosalbutamol tartrate(levalbuterol) is the R-enantiomer of the short-acting β2-adrenergic receptor agonist salbutamol. Levalbuterol tartrate Chemical Structure
  100. GC17653 Levobetaxolol HCl Levobetaxolol HCl is a beta-adrenergic receptor inhibitor (beta blocker) that can lower the pressure in the eye. Levobetaxolol HCl Chemical Structure
  101. GC30972 Lidanserin (ZK-33839) Lidanserin (ZK-33839) (ZK-33839) acts as a 5-HT2A and α1-adrenergic receptor antagonist. Lidanserin (ZK-33839) Chemical Structure

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